# Cetirizine Hydrochloride

NDC: 68071-2571
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20071227

FDA application: ANDA077498

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-2571"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-2571
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d0d8b376-9001-8776-e053-2a95a90ae651